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Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay.
Yeung KS, Ho MSP, Lee SL, Kan ASY, Chan KYK, Tang MHY, Mak CCY, Leung GKC, So PL, Pfundt R, Marshall CR, Scherer SW, Choufani S, Weksberg R, Hon-Yin Chung B. Yeung KS, et al. Among authors: weksberg r. J Med Genet. 2018 Dec;55(12):847-852. doi: 10.1136/jmedgenet-2018-105328. Epub 2018 Jul 14. J Med Genet. 2018. PMID: 30007940
FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.
Teshima I, Chadwick D, Chitayat D, Kobayashi J, Ray P, Shuman C, Siegel-Bartelt J, Strasberg P, Weksberg R. Teshima I, et al. Among authors: weksberg r. Am J Med Genet. 1996 Mar 29;62(3):217-23. doi: 10.1002/(sici)1096-8628(19960329)62:3<216::aid-ajmg3>3.3.co;2-0. Am J Med Genet. 1996. PMID: 8882776
22q11 deletion syndrome in adults with schizophrenia.
Bassett AS, Hodgkinson K, Chow EW, Correia S, Scutt LE, Weksberg R. Bassett AS, et al. Among authors: weksberg r. Am J Med Genet. 1998 Jul 10;81(4):328-37. Am J Med Genet. 1998. PMID: 9674980 Free PMC article.
Phenotype of adults with the 22q11 deletion syndrome: A review.
Cohen E, Chow EW, Weksberg R, Bassett AS. Cohen E, et al. Among authors: weksberg r. Am J Med Genet. 1999 Oct 8;86(4):359-65. doi: 10.1002/(sici)1096-8628(19991008)86:4<359::aid-ajmg10>3.0.co;2-v. Am J Med Genet. 1999. PMID: 10494092 Free PMC article. Review.
Chromosomal abnormalities and schizophrenia.
Bassett AS, Chow EW, Weksberg R. Bassett AS, et al. Among authors: weksberg r. Am J Med Genet. 2000 Spring;97(1):45-51. doi: 10.1002/(sici)1096-8628(200021)97:1<45::aid-ajmg6>3.0.co;2-9. Am J Med Genet. 2000. PMID: 10813803 Free PMC article. Review.
Analphoid 3qter markers.
Teshima I, Bawle EV, Weksberg R, Shuman C, Van Dyke DL, Schwartz S. Teshima I, et al. Among authors: weksberg r. Am J Med Genet. 2000 Sep 11;94(2):113-9. doi: 10.1002/1096-8628(20000911)94:2<113::aid-ajmg3>3.0.co;2-q. Am J Med Genet. 2000. PMID: 10982967
293 results